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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8597676
Species: Homo sapiens
RGD Object: Variant
Symbol: CV22858
Name: NM_000314.8(PTEN):c.388C>T (p.Arg130Ter)
Acc ID: DOID:9002682
Term: Cardiovascular Abnormalities
Definition: Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS.
Definition Source(s): MESH:D018376
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
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